Device recall
Z-0400-05: Powerheart AED G3 Automated External Defibrillator Model 9300P Professional…
FDA device recall · Class II · Cardiac Science, Inc.
Key facts
| Recall number (Z-number) | Z-0400-05 |
|---|---|
| Recall event | 30704 |
| Product | Powerheart AED G3 Automated External Defibrillator Model 9300P Professional series). Cardiac Science AEDs are manufactured by: Manufacturing: Cardiac Science, Inc., 5474 Feltl Road, Minnetonka, MN 55343-7982. |
| Product code | MKJ |
| Recalling firm | Cardiac Science, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2006 |
| 510(k) numbers | K040637 |
| FEI number | 2112020 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database